Canonical Allele Identifier: CA2144022974

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67772109G= , CM000676.2:g.67772109G=	GRCh38
NC_000014.8:g.68238826G= , CM000676.1:g.68238826G=	GRCh37
NC_000014.7:g.67308579G=	NCBI36
NG_011836.1:g.49481C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.5422C= MANE Select	ENSP00000251119.5:p.Gln1808=
ENST00000676512.1:c.5440C=	ENSP00000504552.1:p.Gln1814=
ENST00000676620.1:c.5344C=	ENSP00000504587.1:p.Gln1782=
ENST00000678386.1:c.5467C=	ENSP00000503677.1:p.Gln1823=
ENST00000347230.8:c.5422C=	ENSP00000251119.5:p.Gln1808=
ENST00000554523.5:n.5559C=
ENST00000554557.5:c.*3400C=	ENSP00000450431.1:n.*3400C=
ENST00000555452.1:c.5422C=	ENSP00000450603.1:p.Gln1808=
NM_015346.3:c.5422C=	NP_056161.2:p.Gln1808=
XM_006720093.2:c.5422C=	XP_006720156.1:p.Gln1808=
XM_011536606.1:c.3913C=	XP_011534908.1:p.Gln1305=
XM_011536607.1:c.3097C=	XP_011534909.1:p.Gln1033=
XM_011536608.1:c.3004C=	XP_011534910.1:p.Gln1002=
XM_017021124.1:c.5440C=	XP_016876613.1:p.Gln1814=
XM_017021125.1:c.5440C=	XP_016876614.1:p.Gln1814=
XM_017021126.1:c.3931C=	XP_016876615.1:p.Gln1311=
XM_017021127.2:c.3115C=	XP_016876616.1:p.Gln1039=
XM_017021128.1:c.3022C=	XP_016876617.1:p.Gln1008=
NM_015346.4:c.5422C= MANE Select	NP_056161.2:p.Gln1808=